Process Advantages of Direct CO2 to Methanol Synthesis
Marlin, Dana S., Sarron, Emeric, Sigurbjörnsson, Ómar
Published in Frontiers in chemistry (27.09.2018)
Published in Frontiers in chemistry (27.09.2018)
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Journal Article
Spinal cord neural activity of patients with fibromyalgia and healthy controls during temporal summation of pain: an fMRI study
Staud, Roland, Boissoneault, Jeff, Lai, Song, Mejia, Marlin S, Ramanlal, Riddhi, Godfrey, Melyssa M, Stroman, Patrick W
Published in Journal of neurophysiology (01.09.2021)
Published in Journal of neurophysiology (01.09.2021)
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Journal Article
Mutations in NALP12 cause hereditary periodic fever syndromes
Jéru, I, Duquesnoy, P, Fernandes-Alnemri, T, Cochet, E, Yu, J.W, Lackmy-Port-Lis, M, Grimprel, E, Landman-Parker, J, Hentgen, V, Marlin, S, McElreavey, K, Sarkisian, T, Grateau, G, Alnemri, E.S, Amselem, S
Published in Proceedings of the National Academy of Sciences - PNAS (05.02.2008)
Published in Proceedings of the National Academy of Sciences - PNAS (05.02.2008)
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Journal Article
Spectrum of temporal bone abnormalities in patients with Waardenburg syndrome and SOX10 mutations
Elmaleh-Bergès, M, Baumann, C, Noël-Pétroff, N, Sekkal, A, Couloigner, V, Devriendt, K, Wilson, M, Marlin, S, Sebag, G, Pingault, V
Published in American journal of neuroradiology : AJNR (01.06.2013)
Published in American journal of neuroradiology : AJNR (01.06.2013)
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Journal Article
Nager syndrome: confirmation of SF3B4 haploinsufficiency as the major cause
Petit, F., Escande, F., Jourdain, A.S., Porchet, N., Amiel, J., Doray, B., Delrue, M.A., Flori, E., Kim, C.A., Marlin, S., Robertson, S.P., Manouvrier-Hanu, S., Holder-Espinasse, M.
Published in Clinical genetics (01.09.2014)
Published in Clinical genetics (01.09.2014)
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Journal Article
Heimler Syndrome
Mechaussier, S, Perrault, I, Dollfus, H, Bloch-Zupan, A, Loundon, N, Jonard, L, Marlin, S
Published in Advances in experimental medicine and biology (01.01.2020)
Published in Advances in experimental medicine and biology (01.01.2020)
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Journal Article
Audiological phenotyping evaluation in KBG syndrome: Description of a multicenter review
Rhamati, L., Marcolla, A., Guerrot, A.M., Lerosey, Y., Goldenberg, A., Serey-Gaut, M., Rio, M., Cormier Daire, V., Baujat, G., Lyonnet, S., Rubinato, E., Jonard, L., Rondeau, S., Rouillon, I., Couloignier, V., Jacquemont, M.L., Dupin Deguine, D., Moutton, S., Vincent, M., Isidor, B., Ziegler, A., Marie, J.P., Marlin, S.
Published in International journal of pediatric otorhinolaryngology (01.08.2023)
Published in International journal of pediatric otorhinolaryngology (01.08.2023)
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Journal Article
SOX10 mutations mimic isolated hearing loss
Pingault, V., Faubert, E., Baral, V., Gherbi, S., Loundon, N., Couloigner, V., Denoyelle, F., Noël-Pétroff, N., Ducou Le Pointe, H., Elmaleh-Bergès, M., Bondurand, N., Marlin, S.
Published in Clinical genetics (01.10.2015)
Published in Clinical genetics (01.10.2015)
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Journal Article
Multi-image fusion: optimal decomposition strategy with heuristic-assisted non-subsampled shearlet transform for multimodal image fusion
Ravi, Jampani, Subbayamma, B. V., Kumar, P. Vijaya, Sriramam, Yadavalli S. S., Marlin, S., Sheeba, Adlin, Kumar, N. V. Phani Sai
Published in Signal, image and video processing (01.04.2024)
Published in Signal, image and video processing (01.04.2024)
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Journal Article
Impact of immunological state on eco-physiological variables in one of the southernmost lizards in the world
Duran, Fernando, Boretto, Jorgelina M, Fernández, Jimena B, Molina, Mora Ibáñez, Medina, Marlin S, Ibargüengoytía, Nora R
Published in Anais da Academia Brasileira de Ciências (01.01.2019)
Published in Anais da Academia Brasileira de Ciências (01.01.2019)
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Journal Article
Myopia prevalence and risk factors in children
Theophanous, Christos, Modjtahedi, Bobeck S, Batech, Michael, Marlin, David S, Luong, Tiffany Q, Fong, Donald S
Published in Clinical ophthalmology (Auckland, N.Z.) (01.01.2018)
Published in Clinical ophthalmology (Auckland, N.Z.) (01.01.2018)
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Journal Article
A series of 38 novel germline and somatic mutations of NIPBL in Cornelia de Lange syndrome
Nizon, M., Henry, M., Michot, C., Baumann, C., Bazin, A., Bessières, B., Blesson, S., Cordier-Alex, M.-P., David, A., Delahaye-Duriez, A., Delezoïde, A.-L., Dieux-Coeslier, A., Doco-Fenzy, M., Faivre, L., Goldenberg, A., Layet, V., Loget, P., Marlin, S., Martinovic, J., Odent, S., Pasquier, L., Plessis, G., Prieur, F., Putoux, A., Rio, M., Testard, H., Bonnefont, J.-P., Cormier-Daire, V.
Published in Clinical genetics (01.05.2016)
Published in Clinical genetics (01.05.2016)
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Journal Article
RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa
Moore, A, Escudier, E, Roger, G, Tamalet, A, Pelosse, B, Marlin, S, Clément, A, Geremek, M, Delaisi, B, Bridoux, A-M, Coste, A, Witt, M, Duriez, B, Amselem, S
Published in Journal of medical genetics (01.04.2006)
Published in Journal of medical genetics (01.04.2006)
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Journal Article
IgG4-Related Disease: A New Etiology Underlying Diffuse Intracranial Dilating Vasculopathy
Marlin, Evan S., Dornbos, David, Ikeda, Daniel S., Lehman, Norman L., Powers, Ciarán J.
Published in World neurosurgery (01.11.2017)
Published in World neurosurgery (01.11.2017)
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Journal Article
A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment
del Castillo, F J, Rodríguez-Ballesteros, M, Álvarez, A, Hutchin, T, Leonardi, E, de Oliveira, C A, Azaiez, H, Brownstein, Z, Avenarius, M R, Marlin, S, Pandya, A, Shahin, H, Siemering, K R, Weil, D, Wuyts, W, Aguirre, L A, Martín, Y, Moreno-Pelayo, M A, Villamar, M, Avraham, K B, Dahl, H-H M, Kanaan, M, Nance, W E, Petit, C, Smith, R J H, Van Camp, G, Sartorato, E L, Murgia, A, Moreno, F, del Castillo, I
Published in Journal of medical genetics (01.07.2005)
Published in Journal of medical genetics (01.07.2005)
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Journal Article
Biallelic nonsense mutations in the otogelin-like gene (OTOGL) in a child affected by mild to moderate hearing impairment
Bonnet, C., Louha, M., Loundon, N., Michalski, N., Verpy, E., Smagghe, L., Hardelin, J.-P., Rouillon, I., Jonard, L., Couderc, R., Gherbi, S., Garabedian, E.N., Denoyelle, F., Petit, C., Marlin, S.
Published in Gene (25.09.2013)
Published in Gene (25.09.2013)
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Journal Article
Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90
Roux, A-F, Faugère, V, Le Guédard, S, Pallares-Ruiz, N, Vielle, A, Chambert, S, Marlin, S, Hamel, C, Gilbert, B, Malcolm, S, Claustres, M
Published in Journal of medical genetics (01.09.2006)
Published in Journal of medical genetics (01.09.2006)
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Journal Article